ZMP
si:ch211-66i11.1
Ensembl ID:
ZFIN ID:
Description:
death-associated protein kinase 1 [Source:RefSeq peptide;Acc:NP_001093460]
Human Orthologue:
DAPK1
Human Description:
death-associated protein kinase 1 [Source:HGNC Symbol;Acc:2674]
Mouse Orthologue:
Dapk1
Mouse Description:
death associated protein kinase 1 Gene [Source:MGI Symbol;Acc:MGI:1916885]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33687 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45223 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33688 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14882 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33687
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084314 | Nonsense | 54 | 1439 | 2 | 25 |
ENSDART00000124059 | Nonsense | 54 | 1439 | 3 | 26 |
The following transcripts of ENSDARG00000060093 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46325381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 44106646 |
GRCz11 | 5 | 44706799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGTATGCAGCCAAATTTATCAAGAAGAGGCGGAGCAAATCAAGCCGA[C/T]GAGGGGTCTCAAAAGACGACATTGAGAGGGAGGTCAGCATCCTGAAGGAA
Long Flanking Sequence:
GCTGCTGCTTTAAAAATGACTGACTACTATTAATCTTTTGATCTACTATTTATATACTTTAAAAATAAATGTAGAACACAGTAAAAAAACACTCTAAATCTGTTGAAACACATCGATTTGAAGGCGGTTGTGTTTGTAGCTGGACATTATTGGAGTTCATTGACAGGAACAGTGATCAGCTATTCACTGAAACACCAACAAGTCTCGCTTGATTAACGCAGGACGTTAATTTAGAACAATTTTGACCGCTTGGTTTCACCAATGGCTGTTATTGGGAATGTTTACTGTTCTAAAACATCAGTTGTTTTTATAGTATTATTTCTCAGTTCTTGGCCTTAAAATATGACATATTTCACGTTTTGAATTGGACATGACAGCAATCTTTGTGTTATTGTTTTTTCAGTGGTCAGTTTGCCGTGGTAAAGAAATGCCGTCATAAGAGCACTGGTGTGGAGTATGCAGCCAAATTTATCAAGAAGAGGCGGAGCAAATCAAGCCGA[C/T]GAGGGGTCTCAAAAGACGACATTGAGAGGGAGGTCAGCATCCTGAAGGAAATCCAGCACCCCAATGTCATCACCCTGCACGATGTGTTCGAAAACAAGCATGAAGTCATCCTCATCCTAGAGCTGTGAGTCATTGTTTTTCTCTGCTTTTACTGAATTGTGAAATCACTGACAGCTTTTGTTTGTCTCATTTCTAAAAACTAAAACTGCTGCAGTTATTAGTAGAGGCTAGTAGTATGTGAACAACTGGCTCTTTTAAGTTGTCAAAAGCTCTTCGCTGAATTCAGCAGCACCAGCCTTTACTTACAAAGCAAACACTTGACAAGGTCAACAGTGGGGGGGTAGAGGAGAACCAGTCCATTGAGTAGGTGAACCAGTTTTGCCTGTTGTGCTTTGAACACACATACACTGCTGCCAATGTTTTCAAAGAGAAAAGGCATGTTTTGATGTCTGCACTGTCTTAACTATACTAGTACAGAAGAGTAAGACCTTTGGATGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45223
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084314 | Nonsense | 995 | 1439 | 24 | 25 |
ENSDART00000124059 | Nonsense | 995 | 1439 | 25 | 26 |
The following transcripts of ENSDARG00000060093 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46407489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 44188754 |
GRCz11 | 5 | 44788907 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCGAACCAGCTCATATCATGGCAACAGTTTGTTGTGGATGTGCAAGAA[C/T]AAATCAACCCTCTAGCCAGCGAAGAGGATCTGCGGGGACTGGCTTCACAA
Long Flanking Sequence:
CGATTGTCAATGTATAATTCGCACACTGTTTATATGCCATTTTCAGTGTTATCCACTTAGGAGAGCATCTTTGTAAAAGCTGTGTCTCCACGGGACAAAAAATGGTCTCAGTGGTCATAGAAGGTCAAAACATAAAGGACGATATGTTTATACATATCAAGATTAGTAAGATGTAGCCAAAGGCAGTTAGGGATCTGTTCTTTTGATTTGTCCCACAGAGTAACTACCTAGAAACCACTCAGAATCCCCTAGCAACTGCAAAGAACATGTTAACAACCTCTCAGAAGGACTTGGCAAGCCATTGACAAGCACACGCACACACAGAATATCTCCAGAAATTCAGAAAATACTAATCTTCTTTCTCTCTGTTGTGTTCGCAGACCTGCAGGCCGATGACTCAGCTGGCAGAGAAGCTGTTGTCCACTCTGCCTTCCTGGAGGAAACTGAACGGGCCGAACCAGCTCATATCATGGCAACAGTTTGTTGTGGATGTGCAAGAA[C/T]AAATCAACCCTCTAGCCAGCGAAGAGGATCTGCGGGGACTGGCTTCACAACTTCACAGCATGGGAGAGGTGTGTGTGGGCGGCCCAGAGAAAGTGTCAGATTTTGTGTGTGTGTGTGTGTGCGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACGGTGAGCAGATGAATACATAATTATGCATATTTGAATTATGGGTATAATGCTATTAGTACAAAGGGTGTTTTTGGTGGTTACAGTATTTCAAGCTGTAAACACTAGTATACAGTATACTGTTTTCATGGTACTTATGGTTTTTTATACTGCTTTCTTTTCATTAGTTTCTAGTGCTTGTTCTTTTGGTACTAAGACATTTAAGTTATACATAGATATACGTATAATACATATATACACTCACCACCCACTTTATTAGGTACACCTTACTAGTAATAGAAATTACTAGAAATAGAAATATTCCTCAGAGATTTTGGTCCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33688
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084314 | Nonsense | 1052 | 1439 | 25 | 25 |
ENSDART00000124059 | Nonsense | 1052 | 1439 | 26 | 26 |
The following transcripts of ENSDARG00000060093 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46411545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 44192810 |
GRCz11 | 5 | 44792963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGCTCTGTAGTAACGTACTTGGCAAGCTTCTCTCAATTGAAACCCCC[A/T]AAGCAATCCACCATTATCGCGGCCGATACCGTGTAGAAGAGCTCCAACAC
Long Flanking Sequence:
CTATGGTGGCCATTTTGATGTCGGCCATCTTGGATCCAACTTTTGTTTTTTTAATAGGAAGAGGGTCATTAGACACATCAGACTTATTGGTAATTTCACAAGAAAAACAATGGTGTGCTTGGTTTTAACATAACTTTATTCTTTCATGAGTTATTTACAAGTTTCTGACCACTTAGAAAATGTGTTCAATGTGCTGCCCATTGTGTTGGATTGTCAATGCAACCCTCTTCTCCCACTCTTAACACTGATCGCAACACCGCAGGAGAAATGCCAGCACAGGCTTCCAGTATCTGTAGTTTCAGGTGCTGCACATCTTGTGTCAGCAGAAATTAGCCATTATTGAGAATCTAAGACATTTACTTGTTCTGAATCCTTTGTTTTTTCCTTCTTCCCACCAGATTAACATCATGCAGAGTGAGACAGTCCAAGATGTTGTCCTCTTAGATCCTCGCTGGCTCTGTAGTAACGTACTTGGCAAGCTTCTCTCAATTGAAACCCCC[A/T]AAGCAATCCACCATTATCGCGGCCGATACCGTGTAGAAGAGCTCCAACACCTGGTCTCCGAAGGCGACATCGATGAACTTCTCCAAGTCCTCGACGCCATGGACGTCTGCGCCCGCGACCTGGCCAACCCAGGAATGGTGGACATCCCTGCCCTCATTCGCACAGGTGGCCTGCAGCATACCTGGACAGACGAGGAGGACGTGGAGGGAGAGGACGCTCTGCTTTACGGTGGAGTCCGTATGGTTCCTGTGGAGCACCTGGCACCCTTTCCTTGCGGACTTTTCCATAAGTTACAGGTGAACTTGTGCAGGTGGAGCCGCCAGCAGAAGCCTGAGGTGGAGGCTGATGATGTGAGGTTGTGGAGCGGTGGCGCTCGCATCGGACTTGGTGGTGTGGAGGCTCTGGTTCTGCTTGTGAACCACGGGCAAGGCATGGAGGTACAGTTACGAGGACCTGACACAGATCCGGGACGCTGCTATGCTTTGTTGGACACTCTGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14882
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084314 | Nonsense | 1160 | 1439 | 25 | 25 |
ENSDART00000124059 | Nonsense | 1160 | 1439 | 26 | 26 |
The following transcripts of ENSDARG00000060093 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46411869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 44193134 |
GRCz11 | 5 | 44793287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYGGACTTTTCCATAAGTTACAGGTGAACTTGTGCAGGTGGAGCCGCCAG[C/T]AGAAGCCWGAGGTGGAGGCTGATGAWGTGAGGTTGTGGAGCGGTGGCGCT
Long Flanking Sequence:
AGAAATTAGCCATTATTGAGAATCTAAGACATTTACTTGTTCTGAATCCTTTGTTTTTTCCTTCTTCCCACCAGATTAACATCATGCAGAGTGAGACAGTCCAAGATGTTGTCCTCTTAGATCCTCGCTGGCTCTGTAGTAACGTACTTGGCAAGCTTCTCTCAATTGAAACCCCCAAAGCAATCCACCATTATCGCGGCCGATACCGTGTAGAAGAGCTCCAACACCTGGTCTCCGAAGGCGACATCGATGAACTTCTCCAAGTCCTCGACGCCATGGACGTCTGCGCCCGCGACCTGGCCAACCCAGGAATGGTGGACATCCCTGCCCTCATTCGCACAGGTGGCCTGCAGCATACCTGGACAGACGAGGAGGACGTGGAGGGAGAGGACGCTCTGCTTTACGGTGGAGTCCGTATGGTTCCTGTGGAGCACCTGGCACCCTTTCCTTGCGGACTTTTCCATAAGTTACAGGTGAACTTGTGCAGGTGGAGCCGCCAG[C/T]AGAAGCCTGAGGTGGAGGCTGATGATGTGAGGTTGTGGAGCGGTGGCGCTCGCATCGGACTTGGTGGTGTGGAGGCTCTGGTTCTGCTTGTGAACCACGGGCAAGGCATGGAGGTACAGTTACGAGGACCTGACACAGATCCGGGACGCTGCTATGCTTTGTTGGACACTCTGTGCGGCATGGCTGAGGGTCTGTTAGCTGCTACTTTGCCCGGTTTGCTTACCGCCCGACACTATCTCAGCCCTCAGCAACTGCGTGAACACCACGGCCCAGTCATGCTTTACCAGCCGAGGGACTTTTTTAGAGCTCAAGCGCGAGGTGAGAACGCTCTGTCGAACACCATGGGTGGCTATCGCGAAAGCTTTGTCAGTATCGTAGCATTAGGATGCATTCATGTCTACAAACAGGGCAACCTCGGTGGCGAAGTGGCTGTAGCAGAGGTCAGTCTTTTGGCTCGACGTAAGCTCTGCCGCCTGCTAGACCCGCCTGATGCCCTGGGC
Associated Phenotype:
Not determined